HCID 22609893, compound → HCID 22609913, compound

HRID 2306588Notes

Reaction equation

HRID 2306588 reaction equation
[CH:1]1([C:5]2[C:10]([O:11][CH2:12][C:13]3[N:17](COCC[Si](C)(C)C)[C:16]4[CH:26]=[CH:27][CH:28]=[CH:29][C:15]=4[N:14]=3)=[N:9][N:8]3[C:30]([C:33]4[CH:38]=[CH:37][C:36]([F:39])=[CH:35][C:34]=4[F:40])=[N:31][N:32]=[C:7]3[CH:6]=2)[CH2:4][CH2:3][CH2:2]1>Cl.C(O)C>[NH:17]1[C:16]2[CH:26]=[CH:27][CH:28]=[CH:29][C:15]=2[N:14]=[C:13]1[CH2:12][O:11][C:10]1[C:5]([CH:1]2[CH2:2][CH2:3][CH2:4]2)=[CH:6][C:7]2[N:8]([C:30]([C:33]3[CH:38]=[CH:37][C:36]([F:39])=[CH:35][C:34]=3[F:40])=[N:31][N:32]=2)[N:9]=1

Participants

4

Procedure

A solution of 7-cyclobutyl-3-(2,4-difluorophenyl)-6-[1-(2-trimethylsilanylethoxymethyl)-1H-benzimidazol-2-ylmethoxy]-1,2,4-triazolo[4,3-b]pyridazine (187 mg, 0.333 mmol) in 5M hydrochloric acid (10 ml) and ethanol (4 ml) was heated at 80° C. overnight, then concentrated in vacuo to remove solvents. Saturated potassium carbonate solution was added, then the mixture was diluted with water, filtered and the residual solid washed with water then ether and then dried. The residue was purified by flash chromatography on silica gel using ethyl acetate as eluent to give the title compound (60 mg, 42%). Data for the title compound: 1H NMR (250 MHz, CDCl3) δ 10.62 (1H, br s), 7.85 (2H, m), 7.56 (1H, d, J=1.6 Hz), 7.48 (1H, br s), 7.32 (2H, m), 7.00 (2H, m), 5.65 (2H, s), 3.54 (1H, m), 2.24 (2H, m), 2.01 (3H, m), 1.80 (1H, m); MS (ES+) m/e 433 [MH]+.

Workup

  1. concentrationconcentrated in vacuo
  2. customto remove solvents
  3. additionSaturated potassium carbonate solution was added
  4. additionthe mixture was diluted with water
  5. filtrationfiltered
  6. washthe residual solid washed with water
  7. dry with materialether and then dried
  8. customThe residue was purified by flash chromatography on silica gel

Sources & evidence

ORD record
ord-65465ed91c124b61a66903b232a58480
Source dataset
uspto-grants-2004_12
Patent number
US06828322B2

Reaction notes

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